Please use this identifier to cite or link to this item: http://ir.swu.ac.th/jspui/handle/123456789/14059
Title: Designed construction of recombinant DNA at the ura3Δ0 locus in the yeast Saccharomyces cerevisiae
Authors: Fukunaga T.
Cha-aim K.
Hirakawa Y.
Sakai R.
Kitagawa T.
Nakamura M.
Nonklang S.
Hoshida H.
Akada R.
Keywords: recombinant DNA
article
codon
gene expression
gene locus
gene sequence
gene targeting
nonhuman
open reading frame
polymerase chain reaction
priority journal
Saccharomyces cerevisiae
DNA, Recombinant
Gene Expression Regulation, Fungal
Gene Targeting
Genetic Loci
Homologous Recombination
Polymerase Chain Reaction
Promoter Regions, Genetic
Saccharomyces cerevisiae
Saccharomyces cerevisiae Proteins
Escherichia coli
Saccharomyces cerevisiae
Issue Date: 2013
Abstract: Recombinant DNAs are traditionally constructed using Escherichia coli plasmids. In the yeast Saccharomyces cerevisiae, chromosomal gene targeting is a common technique, implying that the yeast homologous recombination system could be applied for recombinant DNA construction. In an attempt to use a S. cerevisiae chromosome for recombinant DNA construction, we selected the single ura3Δ0 locus as a gene targeting site. By selecting this single locus, repeated recombination using the surrounding URA3 sequences can be performed. The recombination system described here has several advantages over the conventional plasmid system, as it provides a method to confirm the selection of correct recombinants because transformation of the same locus replaces the pre-existing selection marker, resulting in the loss of the marker in successful recombinations. In addition, the constructed strains can serve as both PCR templates and hosts for preparing subsequent recombinant strains. Using this method, several yeast strains that contained selection markers, promoters, terminators and target genes at the ura3Δ0 locus were successfully generated. The system described here can potentially be applied for the construction of any recombinant DNA without the requirement for manipulations in E. coli. Interestingly, we unexpectedly found that several G/C-rich sequences used for fusion PCR lowered gene expression when located adjacent to the start codon. © 2013 John Wiley & Sons, Ltd.
URI: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84878704848&doi=10.1002%2fyea.2957&partnerID=40&md5=cf2a25a8b0ac764182ee8959927fa55f
http://ir.swu.ac.th/jspui/handle/123456789/14059
ISSN: 0749503X
Appears in Collections:SCOPUS 1983-2021

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